Rilpivirine
ATC J05AG05 · 10 markets · 60 records
AU 12 records · 5 strengths
- 25 mgtabletEDURANTJuluca、ODEFSEY
- 900 mg/3 mLinjection · extended-releaseCabenuva
- 900 mginjectionCABENUVA cabotegravir 600 mg/3 mL plus rilpivirine 900 mg/3 mL prolonged-release suspensions for injection vials
- 600 mginjectionCABENUVA cabotegravir 600 mg/3 mL plus rilpivirine 900 mg/3 mL prolonged-release suspensions for injection vials
Records without a stated strength · 1 Cabenuva、EDURANT、Juluca、ODEFSEY、RILPEMVI、TRILPIVI
US 9 records · 2 strengths
- 25 mgtabletCOMPLERAEDURANT、Juluca、ODEFSEY、Manufacturer: Laurus Labs Limited、Manufacturer: Mylan Pharmaceuticals Inc.、Manufacturer: Somerset Therapeutics, LLC
- 2.5 mgtabletEDURANT PED
GB 7 records · 3 strengths
CA 6 records · 2 strengths
EU 6 records · 1 strengths
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
Records without a stated strength · 1 EDURANT、Emtricitabine/Rilpivirine/Tenofovir Alafenamide Viatris、Eviplera 200mg/25mg/245mg tablets、Juluca、ODEFSEY、REKAMBYS
ES 5 records · 3 strengths
- 25 mgtabletEDURANTEviplera 200mg/25mg/245mg tablets、ODEFSEY
- 900 mginjection · extended-releaseREKAMBYS
Records without a stated strength · 1 Juluca
HK 5 records · 1 strengths
Records without a stated strength · 1 EDURANT、ODEFSEY、REKAMBYS PROLONGED-RELEASE SUSPENSION FOR INJECTION 600MG/2ML
TW 4 records · 3 strengths
- 25 mgtabletEDURANT恩臨®膜衣錠25毫克
- 300 mginjection · extended-releaseRekambys prolonged-release suspension for injection 300 mg/mL瑞卡必持續性藥效注射懸浮劑300毫克/毫升
Records without a stated strength · 1 Juluca、ODEFSEY、安以斯膜衣錠、滋若愷膜衣錠
SG 2 records · 2 strengths
- 25 mgtabletODEFSEY
- 300 mg/mLinjection · extended-releaseRekambys prolonged-release suspension for injection 300 mg/mL
MX 1 records · 1 strengths
Records without a stated strength · 1 REKAMBYS
| Strength / form / release | US | GB | CA | AU | SG | ES | MX | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|---|
| 25 mg tablet | Manufacturer: Laurus Labs Limited ×2 Manufacturer: Mylan Pharmaceuticals Inc. Manufacturer: Somerset Therapeutics, LLC | Manufacturer: Gilead Sciences Ltd EDURANT Eviplera 200mg/25mg/245mg tablets | COMPLERA EDURANT Juluca+1ODEFSEY | EDURANT Juluca ODEFSEY | ODEFSEY | EDURANT Eviplera 200mg/25mg/245mg tablets ODEFSEY | EDURANT 恩臨®膜衣錠25毫克 | |||
| 2.5 mg tablet | EDURANT PED | EDURANT | ||||||||
| 900 mg/3 mL injection · extended-release | Rekambys 900mg/3ml prolonged-release suspension for injection vials | Cabenuva | ||||||||
| 300 mg injection · extended-release | Rekambys prolonged-release suspension for injection 300 mg/mL 瑞卡必持續性藥效注射懸浮劑300毫克/毫升 | |||||||||
| 300 mg liquid · extended-release | Cabenuva | |||||||||
| 900 mg injection · extended-release | REKAMBYS | |||||||||
| 900 mg injection | CABENUVA cabotegravir 600 mg/3 mL plus rilpivirine 900 mg/3 mL prolonged-release suspensions for injection vials | |||||||||
| 600 mg injection | CABENUVA cabotegravir 600 mg/3 mL plus rilpivirine 900 mg/3 mL prolonged-release suspensions for injection vials | |||||||||
| 300 mg/mL injection · extended-release | Rekambys prolonged-release suspension for injection 300 mg/mL | |||||||||
unknown | Cabenuva EDURANT Juluca+3ODEFSEY RILPEMVI TRILPIVI | EDURANT ODEFSEY REKAMBYS PROLONGED-RELEASE SUSPENSION FOR INJECTION 600MG/2ML | EDURANT Emtricitabine/Rilpivirine/Tenofovir Alafenamide Viatris Eviplera 200mg/25mg/245mg tablets | |||||||
tablet | Juluca | Juluca ODEFSEY 安以斯膜衣錠+1滋若愷膜衣錠 | ||||||||
liquid | REKAMBYS |
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Each country column shows the locally registered trade names — not translations.
4 more strength/form rows are recorded only in CA · SG · ES · MX and are not shown in this table. Hay 4 filas de concentración/forma registradas solo en CA · SG · ES · MX que no se muestran en esta tabla. 另有 4 个规格/剂型仅在 CA · SG · ES · MX 有记录(未在本表显示)。 另有 4 個規格/劑型僅在 CA · SG · ES · MX 有記錄(未在本表顯示)。
“not disclosed” means the source does not publish the strength — it does not mean the product has none.
Hong Kong records are name/ingredient-level only: no strength, dosage form or registration status; on the register does not prove current supply.
Australia ARTG data has no registration-status column, so status is shown as unknown; being on the register does not mean currently marketed.
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.